Interleukin-6 polymorphism and Helicobacter pylori infection in Brazilian adult patients with chronic gastritis
Helicobacter pylori is recognised as the most common cause of chronic active gastritis and this bacterium is also an important pathogenic factor in peptic ulcer disease. The biological factors that influence clinical outcome in H. pylori infection have been extensively studied. In addition to immuno...
Gespeichert in:
Veröffentlicht in: | Clinical and experimental medicine 2005-10, Vol.5 (3), p.112-116 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 116 |
---|---|
container_issue | 3 |
container_start_page | 112 |
container_title | Clinical and experimental medicine |
container_volume | 5 |
creator | Lobo Gatti, L Zambaldi Tunes, M de Lábio, R W Silva, L C de Arruda Cardoso Smith, M Marques Payão, S L |
description | Helicobacter pylori is recognised as the most common cause of chronic active gastritis and this bacterium is also an important pathogenic factor in peptic ulcer disease. The biological factors that influence clinical outcome in H. pylori infection have been extensively studied. In addition to immunological factors in the host, bacterial virulence determinants in H. pylori strains are likely to play a crucial role in gastric cancer development. Singlenucleotide polymorphisms at the 5' flanking region of the interleukin (IL)-6 gene promoter (G or C at -174 base) have been identified and individuals with the G allele at position -174 have been shown to produce higher levels of IL-6 than those with the C/C genotype. The mucosal levels of IL-6 were reported to be increased in H. pylori-associated gastritis. The present study was conducted to examine any relationship between inflammatory cytokine polymorphisms and the inflammatory process in mucosa infected by H. pylori. In our study we did not find any association between the C and G alleles in adult patients with chronic gastritis and inflammatory process in gastric mucosa. |
doi_str_mv | 10.1007/s10238-005-0074-3 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68796069</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>928086311</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-670f14807c2461141e54150ec8f36b8cf42a63be2a31046bb89e5bcb502059423</originalsourceid><addsrcrecordid>eNqFkc9rFTEQx4NYbK3-AV4keOht7eR39qjF2kLBi55DNi_rS80ma5JFnn-9Ke-B4MXDMHP4fAdmPgi9IfCeAKjrSoAyPQCIXooP7Bm6IGIkwyiofn6atR7hHL2s9RGACM3gBTonkmquGLtA-T41X6LffoQ0SLzmeFhyWfehLtimHb7zMbg8WdcpvB5iLgGHNHvXQk59wh-L_R1isAnb3RYbXm0LPrWKf4W2x25fcgoOf7e1ldBCfYXOZhurf33ql-jb7aevN3fDw5fP9zcfHgbHhGqDVDATrkE5yiUhnHjBiQDv9MzkpN3MqZVs8tQyAlxOkx69mNwkgIIYOWWX6Oq4dy355-ZrM0uozsdok89bNVKrUYIc_wtS6M8kQnXw3T_gY95K6kcYykCBpkJ0iBwhV3Ktxc9mLWGx5WAImCdn5ujMdGfmyZlhPfP2tHibFr_7mzhJYn8Ars2SHg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>230708255</pqid></control><display><type>article</type><title>Interleukin-6 polymorphism and Helicobacter pylori infection in Brazilian adult patients with chronic gastritis</title><source>MEDLINE</source><source>SpringerNature Journals</source><creator>Lobo Gatti, L ; Zambaldi Tunes, M ; de Lábio, R W ; Silva, L C ; de Arruda Cardoso Smith, M ; Marques Payão, S L</creator><creatorcontrib>Lobo Gatti, L ; Zambaldi Tunes, M ; de Lábio, R W ; Silva, L C ; de Arruda Cardoso Smith, M ; Marques Payão, S L</creatorcontrib><description>Helicobacter pylori is recognised as the most common cause of chronic active gastritis and this bacterium is also an important pathogenic factor in peptic ulcer disease. The biological factors that influence clinical outcome in H. pylori infection have been extensively studied. In addition to immunological factors in the host, bacterial virulence determinants in H. pylori strains are likely to play a crucial role in gastric cancer development. Singlenucleotide polymorphisms at the 5' flanking region of the interleukin (IL)-6 gene promoter (G or C at -174 base) have been identified and individuals with the G allele at position -174 have been shown to produce higher levels of IL-6 than those with the C/C genotype. The mucosal levels of IL-6 were reported to be increased in H. pylori-associated gastritis. The present study was conducted to examine any relationship between inflammatory cytokine polymorphisms and the inflammatory process in mucosa infected by H. pylori. In our study we did not find any association between the C and G alleles in adult patients with chronic gastritis and inflammatory process in gastric mucosa.</description><identifier>ISSN: 1591-8890</identifier><identifier>EISSN: 1591-9528</identifier><identifier>DOI: 10.1007/s10238-005-0074-3</identifier><identifier>PMID: 16284733</identifier><identifier>CODEN: CEMLBA</identifier><language>eng</language><publisher>Italy: Springer Nature B.V</publisher><subject>Adult ; Adults ; Bacteria ; Brazil ; Chronic Disease ; Cytokines ; Digestive system ; Female ; Gastritis - genetics ; Gastritis - microbiology ; Gene Frequency ; Helicobacter Infections - genetics ; Helicobacter pylori ; Humans ; Interleukin-6 - genetics ; Male ; Medical disorders ; Polymorphism ; Polymorphism, Genetic ; Polymorphism, Restriction Fragment Length</subject><ispartof>Clinical and experimental medicine, 2005-10, Vol.5 (3), p.112-116</ispartof><rights>Springer-Verlag Italia 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-670f14807c2461141e54150ec8f36b8cf42a63be2a31046bb89e5bcb502059423</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16284733$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lobo Gatti, L</creatorcontrib><creatorcontrib>Zambaldi Tunes, M</creatorcontrib><creatorcontrib>de Lábio, R W</creatorcontrib><creatorcontrib>Silva, L C</creatorcontrib><creatorcontrib>de Arruda Cardoso Smith, M</creatorcontrib><creatorcontrib>Marques Payão, S L</creatorcontrib><title>Interleukin-6 polymorphism and Helicobacter pylori infection in Brazilian adult patients with chronic gastritis</title><title>Clinical and experimental medicine</title><addtitle>Clin Exp Med</addtitle><description>Helicobacter pylori is recognised as the most common cause of chronic active gastritis and this bacterium is also an important pathogenic factor in peptic ulcer disease. The biological factors that influence clinical outcome in H. pylori infection have been extensively studied. In addition to immunological factors in the host, bacterial virulence determinants in H. pylori strains are likely to play a crucial role in gastric cancer development. Singlenucleotide polymorphisms at the 5' flanking region of the interleukin (IL)-6 gene promoter (G or C at -174 base) have been identified and individuals with the G allele at position -174 have been shown to produce higher levels of IL-6 than those with the C/C genotype. The mucosal levels of IL-6 were reported to be increased in H. pylori-associated gastritis. The present study was conducted to examine any relationship between inflammatory cytokine polymorphisms and the inflammatory process in mucosa infected by H. pylori. In our study we did not find any association between the C and G alleles in adult patients with chronic gastritis and inflammatory process in gastric mucosa.</description><subject>Adult</subject><subject>Adults</subject><subject>Bacteria</subject><subject>Brazil</subject><subject>Chronic Disease</subject><subject>Cytokines</subject><subject>Digestive system</subject><subject>Female</subject><subject>Gastritis - genetics</subject><subject>Gastritis - microbiology</subject><subject>Gene Frequency</subject><subject>Helicobacter Infections - genetics</subject><subject>Helicobacter pylori</subject><subject>Humans</subject><subject>Interleukin-6 - genetics</subject><subject>Male</subject><subject>Medical disorders</subject><subject>Polymorphism</subject><subject>Polymorphism, Genetic</subject><subject>Polymorphism, Restriction Fragment Length</subject><issn>1591-8890</issn><issn>1591-9528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkc9rFTEQx4NYbK3-AV4keOht7eR39qjF2kLBi55DNi_rS80ma5JFnn-9Ke-B4MXDMHP4fAdmPgi9IfCeAKjrSoAyPQCIXooP7Bm6IGIkwyiofn6atR7hHL2s9RGACM3gBTonkmquGLtA-T41X6LffoQ0SLzmeFhyWfehLtimHb7zMbg8WdcpvB5iLgGHNHvXQk59wh-L_R1isAnb3RYbXm0LPrWKf4W2x25fcgoOf7e1ldBCfYXOZhurf33ql-jb7aevN3fDw5fP9zcfHgbHhGqDVDATrkE5yiUhnHjBiQDv9MzkpN3MqZVs8tQyAlxOkx69mNwkgIIYOWWX6Oq4dy355-ZrM0uozsdok89bNVKrUYIc_wtS6M8kQnXw3T_gY95K6kcYykCBpkJ0iBwhV3Ktxc9mLWGx5WAImCdn5ujMdGfmyZlhPfP2tHibFr_7mzhJYn8Ars2SHg</recordid><startdate>200510</startdate><enddate>200510</enddate><creator>Lobo Gatti, L</creator><creator>Zambaldi Tunes, M</creator><creator>de Lábio, R W</creator><creator>Silva, L C</creator><creator>de Arruda Cardoso Smith, M</creator><creator>Marques Payão, S L</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>200510</creationdate><title>Interleukin-6 polymorphism and Helicobacter pylori infection in Brazilian adult patients with chronic gastritis</title><author>Lobo Gatti, L ; Zambaldi Tunes, M ; de Lábio, R W ; Silva, L C ; de Arruda Cardoso Smith, M ; Marques Payão, S L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-670f14807c2461141e54150ec8f36b8cf42a63be2a31046bb89e5bcb502059423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>Adults</topic><topic>Bacteria</topic><topic>Brazil</topic><topic>Chronic Disease</topic><topic>Cytokines</topic><topic>Digestive system</topic><topic>Female</topic><topic>Gastritis - genetics</topic><topic>Gastritis - microbiology</topic><topic>Gene Frequency</topic><topic>Helicobacter Infections - genetics</topic><topic>Helicobacter pylori</topic><topic>Humans</topic><topic>Interleukin-6 - genetics</topic><topic>Male</topic><topic>Medical disorders</topic><topic>Polymorphism</topic><topic>Polymorphism, Genetic</topic><topic>Polymorphism, Restriction Fragment Length</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lobo Gatti, L</creatorcontrib><creatorcontrib>Zambaldi Tunes, M</creatorcontrib><creatorcontrib>de Lábio, R W</creatorcontrib><creatorcontrib>Silva, L C</creatorcontrib><creatorcontrib>de Arruda Cardoso Smith, M</creatorcontrib><creatorcontrib>Marques Payão, S L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lobo Gatti, L</au><au>Zambaldi Tunes, M</au><au>de Lábio, R W</au><au>Silva, L C</au><au>de Arruda Cardoso Smith, M</au><au>Marques Payão, S L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interleukin-6 polymorphism and Helicobacter pylori infection in Brazilian adult patients with chronic gastritis</atitle><jtitle>Clinical and experimental medicine</jtitle><addtitle>Clin Exp Med</addtitle><date>2005-10</date><risdate>2005</risdate><volume>5</volume><issue>3</issue><spage>112</spage><epage>116</epage><pages>112-116</pages><issn>1591-8890</issn><eissn>1591-9528</eissn><coden>CEMLBA</coden><abstract>Helicobacter pylori is recognised as the most common cause of chronic active gastritis and this bacterium is also an important pathogenic factor in peptic ulcer disease. The biological factors that influence clinical outcome in H. pylori infection have been extensively studied. In addition to immunological factors in the host, bacterial virulence determinants in H. pylori strains are likely to play a crucial role in gastric cancer development. Singlenucleotide polymorphisms at the 5' flanking region of the interleukin (IL)-6 gene promoter (G or C at -174 base) have been identified and individuals with the G allele at position -174 have been shown to produce higher levels of IL-6 than those with the C/C genotype. The mucosal levels of IL-6 were reported to be increased in H. pylori-associated gastritis. The present study was conducted to examine any relationship between inflammatory cytokine polymorphisms and the inflammatory process in mucosa infected by H. pylori. In our study we did not find any association between the C and G alleles in adult patients with chronic gastritis and inflammatory process in gastric mucosa.</abstract><cop>Italy</cop><pub>Springer Nature B.V</pub><pmid>16284733</pmid><doi>10.1007/s10238-005-0074-3</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1591-8890 |
ispartof | Clinical and experimental medicine, 2005-10, Vol.5 (3), p.112-116 |
issn | 1591-8890 1591-9528 |
language | eng |
recordid | cdi_proquest_miscellaneous_68796069 |
source | MEDLINE; SpringerNature Journals |
subjects | Adult Adults Bacteria Brazil Chronic Disease Cytokines Digestive system Female Gastritis - genetics Gastritis - microbiology Gene Frequency Helicobacter Infections - genetics Helicobacter pylori Humans Interleukin-6 - genetics Male Medical disorders Polymorphism Polymorphism, Genetic Polymorphism, Restriction Fragment Length |
title | Interleukin-6 polymorphism and Helicobacter pylori infection in Brazilian adult patients with chronic gastritis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T14%3A44%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Interleukin-6%20polymorphism%20and%20Helicobacter%20pylori%20infection%20in%20Brazilian%20adult%20patients%20with%20chronic%20gastritis&rft.jtitle=Clinical%20and%20experimental%20medicine&rft.au=Lobo%20Gatti,%20L&rft.date=2005-10&rft.volume=5&rft.issue=3&rft.spage=112&rft.epage=116&rft.pages=112-116&rft.issn=1591-8890&rft.eissn=1591-9528&rft.coden=CEMLBA&rft_id=info:doi/10.1007/s10238-005-0074-3&rft_dat=%3Cproquest_cross%3E928086311%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=230708255&rft_id=info:pmid/16284733&rfr_iscdi=true |